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FDA 510(k)

MS DISPOSABLE RIGID DOPPLER PROBE

K-Number: K930227 · 1993-09-16

ApplicantMeadox Medicals, Div. Boston Scientific Corp.
Decision Date1993-09-16
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MS DISPOSABLE RIGID DOPPLER PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Meadox Medicals, Div. Boston Scientific Corp.. It received FDA 510(k) clearance on 1993-09-16 under 510(k) number K930227. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MS DISPOSABLE RIGID DOPPLER PROBE?

MS DISPOSABLE RIGID DOPPLER PROBE is a medical device that received FDA 510(k) clearance on 1993-09-16. The listed applicant is Meadox Medicals, Div. Boston Scientific Corp.. The 510(k) number is K930227.

When did MS DISPOSABLE RIGID DOPPLER PROBE receive FDA 510(k) clearance?

MS DISPOSABLE RIGID DOPPLER PROBE received FDA 510(k) clearance on 1993-09-16, under 510(k) number K930227.

Who is the listed applicant for MS DISPOSABLE RIGID DOPPLER PROBE?

The FDA 510(k) record lists Meadox Medicals, Div. Boston Scientific Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MS DISPOSABLE RIGID DOPPLER PROBE?

The FDA product code for MS DISPOSABLE RIGID DOPPLER PROBE is DPW.

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Other records listing Meadox Medicals, Div. Boston Scientific Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K953647MS CLASSIQUE BALLOON CATHETER W/HYDROPASS COATINGK960766MEADOX MEDICALS, INC. EXPANDED PTFE VASCULAR GRAFTK962433MEADOX EXXCEL EPTFE VASCULAR GRAFTK961847HEMASHIELD VANTAGE (VASCULAR GRAFTK962342HEMASHIELD FINESSE ULTRA-THIN, KNITTED CARDIOVASCULAR PATCHK955460MEADOX MEDICALS, INC., EXPANDED & EXTERNALLY SUPPORTED EXPANDED PTFE VASCULAR GRAFT

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Related Devices (Code: DPW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260700BlueDop Vascular ExpertBlueDop Medical, Ltd.K252810FloPatch FP120Flosonics MedicalK251904VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-SP-01, VC-SD-01)Remington Medical, Inc.K251114FloPatch FP120Flosonics MedicalK243852Elfor-LElfi-Tech , Ltd.K241583VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-CP-01, VC-CH-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-SP-01, VC-CH-01)Remington Medical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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